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Ziprasidone Hydrochloride - 0904-6271-08 - (Ziprasidone Hydrochloride)

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Drug Information of Ziprasidone Hydrochloride

Product NDC: 0904-6271
Proprietary Name: Ziprasidone Hydrochloride
Non Proprietary Name: Ziprasidone Hydrochloride
Active Ingredient(s): 60    mg/1 & nbsp;   Ziprasidone Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Ziprasidone Hydrochloride

Product NDC: 0904-6271
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077565
Marketing Category: ANDA
Start Marketing Date: 20120315

Package Information of Ziprasidone Hydrochloride

Package NDC: 0904-6271-08
Package Description: 40 CAPSULE in 1 BOX, UNIT-DOSE (0904-6271-08)

NDC Information of Ziprasidone Hydrochloride

NDC Code 0904-6271-08
Proprietary Name Ziprasidone Hydrochloride
Package Description 40 CAPSULE in 1 BOX, UNIT-DOSE (0904-6271-08)
Product NDC 0904-6271
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ziprasidone Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120315
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name ZIPRASIDONE HYDROCHLORIDE
Strength Number 60
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC],Atypical Antipsychotic [EPC]

Complete Information of Ziprasidone Hydrochloride


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